Canonical Allele Identifier: CA2470918999
Gene: KDM5D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19707942C= , CM000686.2:g.19707942C= GRCh38
NC_000024.9:g.21869828C= , CM000686.1:g.21869828C= GRCh37
NC_000024.8:g.20329216C= NCBI36
NG_032920.1:g.41998G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317961.9:c.3391G= MANE Select ENSP00000322408.4:p.Gly1131=
ENST00000317961.8:c.3391G= ENSP00000322408.4:p.Gly1131=
ENST00000382806.6:c.3220G= ENSP00000372256.2:p.Gly1074=
ENST00000415360.1:c.307G= ENSP00000389433.1:p.Gly103=
ENST00000440077.5:c.3268G= ENSP00000398543.1:p.Gly1090=
ENST00000469599.6:n.1989G=
ENST00000492117.1:n.3283G=
ENST00000541639.5:c.3484G= ENSP00000444293.1:p.Gly1162=
NM_001146705.1:c.3484G= NP_001140177.1:p.Gly1162=
NM_001146706.1:c.3220G= NP_001140178.1:p.Gly1074=
NM_004653.4:c.3391G= NP_004644.2:p.Gly1131=
XM_005262560.1:c.3256G= XP_005262617.1:p.Gly1086=
XM_005262561.1:c.3160G= XP_005262618.1:p.Gly1054=
XM_011531468.1:c.3313G= XP_011529770.1:p.Gly1105=
XR_244571.2:n.3679G=
XR_430568.2:n.4013G=
XM_005262560.3:c.3256G= XP_005262617.1:p.Gly1086=
XM_005262561.3:c.3160G= XP_005262618.1:p.Gly1054=
XM_011531468.3:c.3313G= XP_011529770.1:p.Gly1105=
XM_024452495.1:c.1381G= XP_024308263.1:p.Gly461=
XM_024452496.1:c.1147G= XP_024308264.1:p.Gly383=
XR_001756009.2:n.4129G=
XR_001756010.2:n.4129G=
XR_001756011.2:n.3994G=
XR_001756012.2:n.4142G=
XR_001756013.2:n.3460G=
XR_002958832.1:n.3561G=
XR_002958834.1:n.3785G=
XR_002958835.1:n.3668G=
XR_002958836.1:n.4351G=
XR_002958837.1:n.4158G=
XR_244571.4:n.3678G=
XR_430568.4:n.4012G=
NM_001146706.2:c.3220G= NP_001140178.1:p.Gly1074=
NM_004653.5:c.3391G= MANE Select NP_004644.2:p.Gly1131=
NM_001146705.2:c.3484G= NP_001140177.1:p.Gly1162=